Literature DB >> 15481999

Management of acute and chronic gouty arthritis: present state-of-the-art.

Naomi Schlesinger1.   

Abstract

There are three stages in the management of gout: (i) treating the acute attack; (ii) lowering excess stores of uric acid to prevent flares of gouty arthritis and to prevent tissue deposition of urate; and (iii) providing prophylaxis to prevent acute flares. It is important to distinguish between therapy to reduce acute inflammation in acute gout and therapy to manage hyperuricaemia in patients with chronic gouty arthritis. During the acute gouty attack nonpharmacological treatments such as topical ice and rest of the inflamed joint are useful. NSAIDs are the preferred treatment in acute gout. The most important determinant of therapeutic success is not which NSAID is chosen, but rather how soon NSAID therapy is initiated. Other treatments include oral and intravenous colchicine, intra-articular and systemic corticosteroids, and intramuscular corticotropin. Optimal treatment of chronic gout requires long-standing reduction in serum uric acid. The urate-lowering drugs used to treat chronic gout are the uricosuric drugs, the uricostatic drugs, which are xanthine oxidase inhibitors, and the uricolytic drugs. Xanthine oxidase inhibitors such as allopurinol, oxipurinol and febuxastat should be used as first-line treatment in patients with renal calculi, renal insufficiency, concomitant diuretic therapy and ciclosporin (cyclosporine) therapy, and urate overproduction. Uricosuric drugs include probenecid, benzbromarone, micronised fenofibrate and losartan. They are the urate-lowering drugs of choice in allopurinol-allergic patients and underexcretors with normal renal function and no history of urolithiasis. The use of recombinant urate oxidase in patients with chronic gout is limited by the need for parenteral administration, the potential antigenicity and production of anti-urate oxidase antibodies, and declining efficacy. The effectiveness of colchicine prophylaxis as an isolated therapy is still to be confirmed by placebo-controlled trials. Another issue is prophylaxis with NSAIDs. There are no comparative studies with colchicine.

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Year:  2004        PMID: 15481999     DOI: 10.2165/00003495-200464210-00003

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  89 in total

Review 1.  How well have diagnostic tests and therapies for gout been evaluated?

Authors:  N Schlesinger; D G Baker; H R Schumacher
Journal:  Curr Opin Rheumatol       Date:  1999-09       Impact factor: 5.006

2.  Treatment with allopurinol decreases the number of acute gout attacks despite persistently elevated serum uric acid levels.

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Journal:  Clin Exp Rheumatol       Date:  2001 Sep-Oct       Impact factor: 4.473

3.  THE DISTRIBUTION OF SERUM URIC ACID VALUES IN A POPULATION UNSELECTED AS TO GOUT OR HYPERURICEMIA: TECUMSEH, MICHIGAN 1959-1960.

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Journal:  Am J Med       Date:  1965-08       Impact factor: 4.965

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Journal:  Ann Intern Med       Date:  1961-03       Impact factor: 25.391

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Authors:  B T Emmerson
Journal:  N Engl J Med       Date:  1996-02-15       Impact factor: 91.245

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Journal:  Am J Med       Date:  1984-01       Impact factor: 4.965

7.  Asymptomatic hyperuricemia. Risks and consequences in the Normative Aging Study.

Authors:  E W Campion; R J Glynn; L O DeLabry
Journal:  Am J Med       Date:  1987-03       Impact factor: 4.965

Review 8.  Crystal-induced arthritis: an overview.

Authors:  H R Schumacher
Journal:  Am J Med       Date:  1996-02-26       Impact factor: 4.965

9.  Gastrointestinal damage associated with the use of nonsteroidal antiinflammatory drugs.

Authors:  M C Allison; A G Howatson; C J Torrance; F D Lee; R I Russell
Journal:  N Engl J Med       Date:  1992-09-10       Impact factor: 91.245

10.  Effectiveness of etodolac ('Lodine') compared with naproxen in patients with acute gout.

Authors:  A Maccagno; E Di Giorgio; A Romanowicz
Journal:  Curr Med Res Opin       Date:  1991       Impact factor: 2.580

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  37 in total

1.  Effect of hydrochlorothiazide on the pharmacokinetics and pharmacodynamics of febuxostat, a non-purine selective inhibitor of xanthine oxidase.

Authors:  Brian Grabowski; Reza Khosravan; Jing-Tao Wu; Laurent Vernillet; Christopher Lademacher
Journal:  Br J Clin Pharmacol       Date:  2010-07       Impact factor: 4.335

Review 2.  Gout in solid organ transplantation: a challenging clinical problem.

Authors:  Lisa Stamp; Martin Searle; John O'Donnell; Peter Chapman
Journal:  Drugs       Date:  2005       Impact factor: 9.546

Review 3.  Difficult-to-treat gouty arthritis: a disease warranting better management.

Authors:  Naomi Schlesinger
Journal:  Drugs       Date:  2011-07-30       Impact factor: 9.546

Review 4.  Therapeutic effects of xanthine oxidase inhibitors: renaissance half a century after the discovery of allopurinol.

Authors:  Pál Pacher; Alex Nivorozhkin; Csaba Szabó
Journal:  Pharmacol Rev       Date:  2006-03       Impact factor: 25.468

5.  Single-dose, open-label study of the differences in pharmacokinetics of colchicine in subjects with renal impairment, including end-stage renal disease.

Authors:  Suman Wason; David Mount; Robert Faulkner
Journal:  Clin Drug Investig       Date:  2014-12       Impact factor: 2.859

Review 6.  Pathophysiology, clinical presentation and treatment of gout.

Authors:  Gim Gee Teng; Raj Nair; Kenneth G Saag
Journal:  Drugs       Date:  2006       Impact factor: 9.546

Review 7.  Febuxostat for treating chronic gout.

Authors:  Jean H Tayar; Maria Angeles Lopez-Olivo; Maria E Suarez-Almazor
Journal:  Cochrane Database Syst Rev       Date:  2012-11-14

Review 8.  Beyond Joints: a Review of Ocular Abnormalities in Gout and Hyperuricemia.

Authors:  Yael Sharon; Naomi Schlesinger
Journal:  Curr Rheumatol Rep       Date:  2016-06       Impact factor: 4.592

Review 9.  Systemic corticosteroids for acute gout.

Authors:  H J E M Janssens; P L B J Lucassen; F A Van de Laar; M Janssen; E H Van de Lisdonk
Journal:  Cochrane Database Syst Rev       Date:  2008-04-16

10.  Urinary L-type fatty acid-binding protein can reflect renal tubulointerstitial injury.

Authors:  Tamami Tanaka; Kent Doi; Rui Maeda-Mamiya; Kousuke Negishi; Didier Portilla; Takeshi Sugaya; Toshiro Fujita; Eisei Noiri
Journal:  Am J Pathol       Date:  2009-03-05       Impact factor: 4.307

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